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rs9267665

From SNPedia

Orientationplus
Stabilizedplus
Make rs9267665(C;C)
Make rs9267665(C;T)
Make rs9267665(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31903079
GeneC2, ZBTB12
is asnp
is mentioned by
dbSNPrs9267665
dbSNP (classic)rs9267665
ClinGenrs9267665
ebirs9267665
HLIrs9267665
Exacrs9267665
Gnomadrs9267665
Varsomers9267665
LitVarrs9267665
Maprs9267665
PheGenIrs9267665
Biobankrs9267665
1000 genomesrs9267665
hgdprs9267665
ensemblrs9267665
geneviewrs9267665
scholarrs9267665
googlers9267665
pharmgkbrs9267665
gwascentralrs9267665
openSNPrs9267665
23andMers9267665
SNPshotrs9267665
SNPdbers9267665
MSV3drs9267665
GWAS Ctlgrs9267665
GMAF0.07622
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21764829]
Trait
Title A genome-wide association study of hepatitis B vaccine response in an Indonesian population reveals multiple independent risk variants in the HLA region.
Risk Allele
P-val 1E-17
Odds Ratio 2.0500 [1.64-2.57]


[PMID 29283494] Genetic association of complement component 2 variants with chronic hepatitis B in a Korean population.